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About the role
Alimentiv seeks a remote, full-time, one-year limited-term Clinical Project Manager for imaging clinical research projects. The role manages project planning, protocols, risks, resources, documents, timelines, multidisciplinary teams, sponsor liaison, regulatory compliance, reporting, and client support. Applicants need one to three years of related experience and a three-year college advanced diploma/degree in a relevant field; health sciences or clinical research is preferred. Imaging experience is an asset.
Key requirements
Employer-stated requirements where available.
• Applicants should have a minimum of one to three years of related work experience with ongoing training, and a three-year College Advance Diploma/Degree in a relevant field of study, preferable in (Health) Sciences or Clinical Research.
• At least 1 year of relevant experience
• Required skills: clinical research project management, project planning and execution, risk management, regulatory compliance, multidisciplinary team management, sponsor liaison and client support, strong communication, attention to detail, teamwork
Opportunity details
• Workplace: Remote
• Employment: Temporary
• Posted: Sep 1, 2026
• Original advert language: English
Full vacancy
Read the employer’s full description
Job title: Imaging Clinical Project Manager (1 -Year Limited Term)
Department: Medical Imaging
Team: Imaging Project Management
Location: London, Ontario
All locations: London, Ontario, Calgary, Alberta, Edmonton, Alberta, Halifax, Nova Scotia, Kingston, Ontario, Kitchener, Ontario, Montreal, Quebec, Ottawa, Ontario, Quebec City, Quebec, Sherbrooke, Quebec, St. Catherines, Ontario, Toronto, Ontario, Victoria, British Columbia, Vancouver, British Columbia, Windsor, Ontario
Work type: Full-time, Limited term
Workplace type: remote
As the primary sponsor liaison and advocate, the Clinical Project Manager will plan, execute, manage and monitor regional, single modality or therapeutic area clinical research projects. Utilizing existing templates, processes and programs as a guide, he or she will adapt/develop, implement, monitor and be accountable for project protocols, operational plans, risk management, resources, project tools/materials, documents and timelines. The successful candidate will be managing the day to day activities and performance of a multidisciplinary project team, ensuring all decisions align with corporate, industry, sponsor and regulatory requirements.
Project Management
Manage the planning, execution, progress and completion of assigned clinical research projects.
Work with functional experts to ensure all project activities comply with applicable regulations, guidelines, and corporate policies.
Maintain operational, financial and regulatory integrity and safety.
Develop and/or participate in the development of project communications, training, regulatory submissions and/or audits and selection of third party vendors as required.
Documents and Tools
Manage a cross-functional team to ensure the appropriate creation, delivery, maintenance and disposal of all related data, documents, equipment and tools, including protocols, SOPs, informed consent forms, case report forms and instructions.
Prepare investigator updates and other project related reports as required to support the proper conduct and execution throughout the life cycle of assigned projects.
Project Team Performance
Identify, assign and monitor the completion of interdisciplinary project tasks that include site monitoring, CRF and database development and revision, data collection, patient safety/adverse event management, document management, statistical analysis and/or final report writing and publications.
Ensure task completion performance meets or exceeds quality standards and sponsor/client, project and regulatory expectations and guidelines.
Client/Sponsor Support
Act as primary liaison throughout the project life cycle ensuring client/sponsor expectations are appropriately managed by addressing and resolving queries/issues, planning and executing all project meetings, assisting with site and patient recruitment strategies and materials, assisting with the development of stakeholder training and by regularly providing sponsor/client with project status and update reports.
Qualifications
Applicants should have a minimum of one to three years of related work experience with ongoing training, and a three-year College Advance Diploma/Degree in a relevant field of study, preferable in (Health) Sciences or Clinical Research.
Experience within Imaging is an asset
The successful candidate must exhibit the following skills: self-motivation with strong communication skills and a commitment to achieving positive results.
Strong attention to detail and keenness to understand the importance of building collaborative relationships to achieve results.
Ability to engage in continuous learning and self-development.
Ability to continually foster teamwork.
Working Conditions
Home Based
Occasional travel
*Accommodations for job applicants with disabilities are available upon request
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HealthRoleIQ summarises the verified facts needed for matching. Complete responsibilities, project background and employer benefits remain available on the original employer posting.